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Synergetics 56.00.25P

by Synergetics USA, Inc.

Synergetics 56.00.25P is a Class II device made by Synergetics USA, Inc., listed in FDA GUDID since 19 Aug 2016 (UDI-DI 20841305108039), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20841305108039 UDI-DI Date19 Aug 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Synergetics
Generic name
Electrosurgical system
Model / Ref / Catalog
56.00.25P
Primary DI / UDI-DI
20841305108039
FDA product code
HQR
GMDN term
Electrosurgical system
Device class
Class II
Regulation number
886.4100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrosurgical system

Similar devices in this category

Other devices filed under Electrosurgical system.

Other devices from Synergetics, Inc.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)